FDA 510(k)

XOD Diathermia Radiofrequency Device

Número K: K242175 · 2025-02-27

Data da decisão2025-02-27

Código do produtoPBX

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

XOD Diathermia Radiofrequency Device is the device name listed in this FDA 510(k) record. The listed applicant is Xod, Inc.. It received FDA 510(k) clearance on 2025-02-27 under 510(k) number K242175. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the XOD Diathermia Radiofrequency Device?

XOD Diathermia Radiofrequency Device is a medical device that received FDA 510(k) clearance on 2025-02-27. The listed applicant is Xod, Inc.. The 510(k) number is K242175.

When did XOD Diathermia Radiofrequency Device receive FDA 510(k) clearance?

XOD Diathermia Radiofrequency Device received FDA 510(k) clearance on 2025-02-27, under 510(k) number K242175.

Who is the listed applicant for XOD Diathermia Radiofrequency Device?

The FDA 510(k) record lists Xod, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XOD Diathermia Radiofrequency Device?

The FDA product code for XOD Diathermia Radiofrequency Device is PBX.

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